Department of Prosthodontics and Implant Innovation, University of Illinois at Chicago, College of Dentistry, Chicago, Illinois.
Department of Oral Medicine and Diagnostic Sciences, College of Dentistry, University of Illinois at Chicago, Chicago, Illinois.
Oral Dis. 2019 Apr;25(3):911-918. doi: 10.1111/odi.13039. Epub 2019 Feb 10.
Measurement of saliva microbes is promoted as a way to detect oral and systemic disease, yet there is a multitude of factors that affect the oral microbiome. The salivary microbiome is influenced by oral biofilm of shedding (epithelial) and non-shedding (tooth) surfaces.
To gauge the ability of salivary microbial analytics to distinguish between edentulous and dentate oral conditions, we looked for differences in the saliva microbiome of subjects with and without teeth. Fifty-two dentate and 49 edentulous subjects provided stimulated saliva samples. 16S rRNA gene sequencing, QIIME-based data processing, and statistical analysis were done using several different analytical approaches to detect differences in the salivary microbiome between the two groups.
Bacteria diversity was lower in the edentulous group. Remarkably, all 31 of the most significant differences in taxa were deficits that occur in the edentulous group. As one might expect many of these taxa are attributed to dental plaque and gingival sulcus associated bacteria.
In sum, the measurement of 16S rRNA genes in the bacteria of the saliva can be used to reproducibly measure differences in the oral microbiome that occur with edentulism, mainly the lack of tooth and tooth-related structures.
测量唾液微生物被推广为一种检测口腔和全身疾病的方法,但有许多因素会影响口腔微生物组。唾液微生物组受脱落(上皮)和非脱落(牙齿)表面的口腔生物膜影响。
为了评估唾液微生物分析在区分无牙和有牙口腔状况方面的能力,我们寻找了有牙和无牙受试者唾液微生物组之间的差异。52 名有牙和 49 名无牙受试者提供了刺激唾液样本。使用几种不同的分析方法进行 16S rRNA 基因测序、基于 QIIME 的数据分析和统计分析,以检测两组唾液微生物组之间的差异。
无牙组的细菌多样性较低。值得注意的是,在分类群中,有 31 个最显著的差异都是无牙组中出现的缺陷。正如人们可能预期的那样,许多这些分类群归因于牙菌斑和牙龈沟相关细菌。
总之,16S rRNA 基因在唾液细菌中的测量可用于可重复地测量无牙状态下发生的口腔微生物组差异,主要是由于缺乏牙齿和与牙齿相关的结构。